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Member InformationCarl June, MD Office Phone: 215-573-5745 Education: MD 1979, Baylor College of Medicine Keywords: Immunotherapy, lymphocyte activation Research and/or Clinical Interests: Summary: Over the last five years my laboratory has been studying the potential use of adoptive immunotherapy for HIV infection. We have developed a large-scale tissue culture technique that permits the efficient propagation of polyclonal HIV CD4 and CD8 T cells from patients with HIV infection. Several clinical trials involving adoptive immunotherapy of autologous and allogeneic T cells are in process. Other trials involve infusions of gene modified T cells. Another project in my laboratory involves determining mechanisms of T cell signal transduction. For the past ten years these studies have been focused on CD28 and CTLA-4. More recently we have also been studying mechanisms that regulate chemokine receptor expression and signal transduction in T cells. In addition, we have studied the role of telomerase expression, telomere maintenance and replicative senescence in T cells. Representative Publications: Levine,B.L., Mosca,J., Riley,J.L., Carroll,R.G., Vahey,M.T., Jagodizinski,L., Wagner,K.F., Mayers,D.L., Burke,D.S., Weislow,O.S. and June C.H.. 1996. Antiviral Effect and Ex Vivo CD4+ T Cell Proliferation In HIV-Positive Patients as a Result of CD28 Costimulation. Science 272:1939-1943. Levine,B.L., Mosca,J., Riley,J.L., Carroll,R.G., Vahey,M.T., Jagodizinski,L., Wagner,K.F., Mayers,D.L., Burke,D.S., Weislow,O.S. et al. 1996. Antiviral Effect and Ex Vivo CD4+ T Cell Proliferation In HIV-Positive Patients as a Result of CD28 Costimulation. Science 272:1939-1943. Riley,J.L., Schlienger,K., Blair PB, Carreno,B.M., Craighead,N., Kim,D., Carroll,R.G., and June C.H. 2000. Modulation of Susceptibility to HIV-1Infection by the Cytotoxic T Lymphocyte Antigen 4 Costimulatory Molecule. J Exp Medicine 191:1987-1998. Levine,B.L., Bernstein WB, Aronson NE, Schlienger K, Cotte J, Perfetto S, Humphries MJ, Ratto-Kim S, Birx DL, Steffans C and June CH . 2002. Adoptive Transfer of Costimulated CD4 + T cells Induces Expansion of Peripheral T Cells and Decreased CCR5 Expression in HIV Infection. Nature. Med. 8:47-53. Riley, J. L., B. L. Levine, N. Craighead, T. Francomano, D. Kim, R. G. Carroll, and C. H. June. Naive and memory CD4 T cells differ in their susceptibility to HIV-1 infection following CD28 costimulation: Implications for transmission and pathogenesis. J Virol. 72:8273-8280, 1998. Ward, S. G., and C. H. June. T lymphocyte activation. In: Encyclopedia of Immunology, edited by I. M. Roitt and P. J. Delves, London : Academic Press, 1999, p. 2323-2329. Levine, B. L., J. Mosca, J. L. Riley, R. G. Carroll, M. T. Vahey, L. Jagodizinski, K. F. Wagner, D. L. Mayers, D. S. Burke, O. S. Weislow, D. C. St.Louis, and C. H. June. Antiviral Effect and Ex Vivo CD4+ T Cell Proliferation In HIV-Positive Patients as a Result of CD28 Costimulation. Science 272:1939-1943, 1996. Blair, P. J., J. L. Riley, B. L. Levine, K. P. Lee, N. Craighead, T. Francomano, S. J. Perfetto, G. S. Gray, B. M. Carreno, and C. H. June. CTLA-4 Ligation Delivers a Unique Signal to Resting CD4 T Cells that Promotes Cell Survival but not IL-2 Secretion. J Immunol 160:12-15, 1998. 1997. Kaushal, S., A. L. Landay, M. Lederman, E. Connick, J. Spritzler, D. R. Kuritzkes, H. Kessler, B. L. Levine, D. St.Louis, and C. H. June. Increases in T-cell telomere length in HIV infection after antiretroviral combination therapy for HIV-1 infection implicate distinct population dynamics in CD4+ and CD8+ T-cells. Clinical Immunology 92:14-24, 1999. |
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